| No. |
Year |
Title |
Author |
Corresponding |
Journal |
Vol. |
Pages |
| 1 |
2013 |
De novo mutations in the autophagy gene encoding WDR45 cause static encephalopathy of childhood with neurodegeneration in adulthood. |
Saitsu H, Nishimura T, Muramatsu K, Kodera H, Kumada S, Sugai K, Kasai-Yoshida E, Sawaura N, Nishida H, Hoshino A, Ryujin F, Yoshioka S, Nishiyama K, Kondo Y, Tsurusaki Y, Nakashima M, Miyake N, Arakawa H, Kato M, Mizushima N, Matsumoto N. |
Saitsu H, Nishimura T, Muramatsu K |
Nature Genetics |
45(4) |
445-449 |
| 2 |
2013 |
The landscape of somatic mutations in Down syndrome-related myeloid disorders. |
Yoshida K, Toki T, Okuno Y, Kanezaki R, Shiraishi Y, Sato-Otsubo A, Sanada M, Park MJ, Terui K, Suzuki H, Kon A, Nagata Y, Sato Y, Wang R, Shiba N, Chiba K, Tanaka H, Hama A, Muramatsu H, Hasegawa D, Nakamura K, Kanegane H, Tsukamoto K, Adachi S, Kawakami K, Kato K, Nishimura R, Izraeli S, Hayashi Y, Miyano S, Kojima S, Ito E, Ogawa S. |
Ogawa S, Ito E |
Nature Genetics |
45(11) |
1293-1299 |
| 3 |
2013 |
An empirical Bayesian ework for somatic mutation detection from cancer genome sequencing data. |
Shiraishi Y, Sato Y, Chiba K, Okuno Y, Nagata Y, Yoshida K, Shiba N, Hayashi Y, Kume H, Homma Y, Sanada M, Ogawa S, Miyano S. |
Shiraishi Y |
Nucleic Acids Res |
41(7) |
e89 |
| 4 |
2013 |
NUP98-NSD1 gene fusion and its related gene xpression signature are strongly associated with a poor prognosis in pediatric acute myeloid leukemia. |
Shiba N, Ichikawa H, Taki T, Park MJ, Jo A, Mitani S, Kobayashi T, Shimada A, Sotomatsu M, Arakawa H, Adachi S, Tawa A, Horibe K, Tsuchida M, Hanada R, Tsukimoto I, Hayashi Y. |
Hayashi Y |
Genes Chromosomes Cancer |
52(7) |
683-693 |
| 5 |
2013 |
Wiskott–Aldrich syndrome presenting with a clinical picture mimicking juvenile myelomonocytic leukaemia. |
Yoshimi A, Kamachi Y, Imai K, Watanabe N, Nakadate H, Kanazawa T, Ozono S, Kobayashi R, Yoshida M, Kobayashi C, Hama A, Muramatsu H, Sasahara Y, Jakob M, Morio T, Ehl S, Manabe A, Niemeyer C, Kojima S. |
Yoshimi A |
Pediatr Blood Cancer |
60(5) |
836-841 |
| 6 |
2013 |
Complications of peripherally inserted central venous catheter in Japanese neonatal intensive care units. |
Ohki Y, Maruyama K, Harigaya A, Kohno M, Arakawa H. |
Ohki Y |
Pediatr Int |
55(2) |
185-189 |
| 7 |
2013 |
Efficacy of Intravenous Immunoglobulin Combined with Prednisolone Following Resistance to Initial Intravenous Immunoglobulin Treatment of Acute Kawasaki Disease. |
Kobayashi T, Kobayashi T, Morikawa A, Ikeda K, Seki M, Shimoyama S, Ishii Y, Suzuki T, Nakajima K, Sakamoto N, Arakawa H. |
Kobayashi T |
J Pediatr |
163 |
521-526 |
| 8 |
2013 |
Flow-adjustable bilateral pulmonary artery banding in the neonatal period for severe congenital heart diseases. |
Yoshimoto A, Miyamoto T, Ozaki S, Kobayashi T, Kobayashi T. |
Yoshimoto A |
Gen Thorac Cardiovasc Surg |
61 |
340-344 |
| 9 |
2013 |
Pulmonary arterial wall stiffness and its impact on right ventricular afterload in patients with repaired tetralogy of fallot. |
Inuzuka R, Seki M, Sugimoto M, Saiki H, Masutani S, Senzaki H. |
Senzaki H |
Ann Thorac Surg |
96 |
1435-1441 |
| 10 |
2013 |
‘I-shaped’ sign in the upper mediastinum: a novel potential marker for antenatal diagnosis of d-transposition of the great arteries. |
Ishii Y, Inamura N, Kawazu Y, Kayatani F, Arakawa H. |
Ishii Y |
Ultrasound Obstet Gynecol |
41 |
667–671 |
| 11 |
2014 |
Progressive aortic dilation and aortic stiffness in children with repaired tetralogy of Fallot. |
Seki M, Kurishima C, Saiki H, Masutani S, Arakawa H, Tamura M, Senzaki H. |
Senzaki H |
Heart Vessels |
29(1) |
83-87 |
| 12 |
2014 |
Mutations of the GATA2 and CEBPA genes in paediatric acute myeloid leukaemia. |
Shiba N, Funato M, Ohki K, Park MJ, Mizushima Y, Adachi S, Kobayashi M, Kinoshita A, Sotomatsu M, Arakawa H, Tawa A, Horibe K, Tsukimoto I, Hayashi Y. |
Hayashi Y |
Br J Haematol |
164(1) |
142–145 |
| 13 |
2014 |
SETBP1 mutations in juvenile myelomonocytic leukaemia and myelodysplastic syndrome but not in paediatric acute myeloid leukaemia. |
Shiba N, Ohki K, Park MJ, Sotomatsu M, Kudo K, Ito E, Sako M, Arakawa H, Hayashi Y. |
Hayashi Y |
Br J Haematol |
164(1) |
156–159 |
| 14 |
2014 |
Glucose promotes its own metabolism by acting on the cell-surface glucose-sensing receptor T1R3. |
Nakagawa Y, Ohtsu Y, Nagasawa M, Shibata H, Kojima I. |
Kojima I |
Endocr J |
61(2) |
119-131 |
| 15 |
2014 |
Reference values for Japanese children’s respiratory resistance using the LMS method. |
Hagiwara S, Mochizuki H, Muramatsu R, Koyama H, Yagi H, Nishida Y, Kobayashi T, Sakamoto N, Takizawa T, Arakawa H. |
Satomi Hagiwara, Takumi Takizawa |
Allergol Int |
63(1) |
113-119 |
| 16 |
2014 |
Sweet Taste-sensing Receptor Expressed in Pancreatic bete-cells: Sweet Molecules Act as Biased Agonists |
Kojima I, Nakagawa Y, Ohtsu Y, Medina A, Nagasawa M. |
Kojima I |
Diabetes Metab J |
29(1) |
12-19 |
| 17 |
2014 |
Diverse signaling systems activated by the sweet taste receptor in human GLP-1-secreting cells. |
Ohtsu Y, Nakagawa Y, Nagasawa M, Arakawa H, Kojima I. |
Kojima I |
Molecular and Cellular Endcrinology |
394(1-2) |
70-79 |
| 18 |
2014 |
Evaluation of bilateral pulmonary artery banding for initial palliation in single-ventricle neonates and infants: risk factors for mortality before the bidirectional Glenn procedure |
Ishii Y. Inamura N, Kayatani F, Iwai S, Kawata H, Arakawa H, Kishimoto H. |
Ishii Y |
Interact Cardiovasc Thorac Surg |
19(5) |
807-811 |
| 19 |
2014 |
Efficacy of the circulatory management of an antenatally diagnosed congenital diaphragmatic hernia: outcomes of the proposed strategy. |
Inamura N,Kubota A, Ishii R, Ishii Y, Kawazu Y, Hamamichi Y, Yoneda A, Kawahara H, Okuyama H, Kayatani F. |
Inamura N |
Pediatr Surg Int |
30(9) |
889-894 |
| 20 |
2014 |
Rupture of a coronary artery aneurysm in Kawasaki disease: a rare case and review of the literature for the past 15 years |
Miyamoto T, Ikeda K, Ishii Y, Kobayashi T. |
Miyamoto T |
J Thorac Cardiovasc Surg |
147(6) |
67 |
| 21 |
2014 |
Foxa2 acts as a co-activator potentiating expression of the Nurr1-induced DA phenotype via epigenetic regulation |
Yi SH. He XB, Rhee YH, Park CH, Takizawa T, Nakashima K, Lee SH. |
Lee SH |
Development |
141(4) |
761-772 |
| 22 |
2014 |
Combination of postmortem mass spectrometry imaging and genetic analysis reveals very long-chain acyl-CoA dehydrogenase deficiency in a case of infant death with liver steatosis |
Takahashi Y, Sano R, Nakajima T, Kominato Y, Kubo R, Takahashi K, Ohshima N, Hirano T, Kobayashi S, Shimada T, Tokue H, Awata S, Hirasawa S, Ishige T. |
Kominato Y |
Forensic Sci Int |
244 |
e34-37 |
| 23 |
2015 |
Endoscopic Findings in the Acute Phase of Food Protein-induced Enterocolitis Syndrome |
Ishige T, Yagi H,Tatsuki M, Hatori R,Nishida Y, Takizawa T,Arakawa H. |
Ishige T |
Pediatr Allergy Immunol |
26(1) |
90-91 |
| 24 |
2015 |
Return of the glucoreceptor: Glucose activates the glucose-sensing receptor T1R3 and facilitates metabolism in pancreatic β-cells. |
Kojima I, Nakagawa Y, Ohtsu Y, Hamano K, Medina J, Nagasawa M. |
Kojima I |
Journal of Diabetes Investigation |
6(3) |
256–263 |
| 25 |
2016 |
Congenital nephrotic syndrome with a novel NPHS1 mutation. |
Yoshizawa C, Kobayashi Y, Ikeuchi Y, Tashiro M, Kakegawa S, Watanabe T, Goto Y, Nakanishi K, Yoshikawa N, Arakawa H. |
Kobayashi Y |
Pediatr Int. |
58(11) |
1211-1215 |
| 26 |
2016 |
SAMD9 mutations cause a novel multisystem disorder, MIRAGE syndrome, and are associated with loss of chromosome 7. |
Narumi S, Amano N, Ishii T, Katsumata N, Muroya K, Adachi M, Toyoshima K, Tanaka Y, Fukuzawa R, Miyako K, Kinjo S, Ohga S, Ihara K, Inoue H, Kinjo T, Hara T, Kohno M, Yamada S, Urano H, Kitagawa Y, Tsugawa K, Higa A, Miyawaki M, Okutani T, Kizaki Z, Hamada H, Kihara M, Shiga K, Yamaguchi T, Kenmochi M, Kitajima H, Fukami M, Shimizu A, Kudoh J, Shibata S, Okano H, Miyake N, Matsumoto N, Hasegawa T. |
Hasegawa T |
Nat Genet |
48(7) |
792-7 |
| 27 |
2016 |
Sucralose, an activator of the glucose-sensing receptor, increases ATP by calcium-dependent and -independent mechanisms |
Li L, Ohtsu Y, Nakagawa Y, Masuda K, Kojima I. |
Kojima I |
Endocr J |
63(8) |
715-25 |
| 28 |
2016 |
Variations in ORAI1 Gene Associated with Kawasaki Disease. |
Onouchi Y, Fukazawa R, Yamamura K, Suzuki H, Kakimoto N, Suenaga T, Takeuchi T, Hamada H, Honda T, Yasukawa K, Terai M, Ebata R, Higashi K, Saji T, Kemmotsu Y, Takatsuki S, Ouchi K, Kishi F, Yoshikawa T, Nagai T, Hamamoto K, Sato Y, Honda A, Kobayashi H, Sato J, Shibuta S, Miyawaki M, Oishi K, Yamaga H, Aoyagi N, Yoshiyama M, Miyashita R, Murata Y, Fujino A, Ozaki K, Kawasaki T, Abe J, Seki M, Kobayashi T, Arakawa H, Ogawa S, Hara T, Hata A, Tanaka T. |
Onouchi Y |
PLoS One. |
11(1) |
e0145486 |
